A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4752655



Internal ID20528515
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:55446364..55446364hg38UCSC Ensembl
chr12:55840148..55840148hg19UCSC Ensembl
Cytoband12q13.2
Allele length
AssemblyAllele length
hg38231
hg19231
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16285935
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4752655
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer